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Dominic V. McGrath, G. Dana Brabson, K. Barry Sharpless, and Lester Andrews. Inorg. Chem. , 1993, 32 (19), pp 4164–4165. DOI: 10.1021/ic00071a035...
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Inorg. Chem. 1993,32, 4164-4165

4164

Reinvestigation of the Infrared Spectra of Oxoosmium(M) Esters by Isotopic Labeling

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Dominic V. McGrath,t G. Dana Bra-* K. Barry Sharplem,'st and Lester Andrews'** Departments of Chemistry, The Scripps Research Institute, La Jolla, California 92037, and University of Virginia, Charlottesville, Virginia 2290 1

Received June 22, I993 As part of our efforts to probe the mechanism of the osmylation reaction' using matrix isolation techniques in concert with infrared spectroscopy,2 we have reinvestigated the infrared spectrum of the oxoosmium(V1) ester complex of 2,3-dimethyl-2-butene (tetramethylethylene, TME). We have found discrepancies in our interpretation of the isotopic data with the assignments made in theliterat~re.~ Thisshort note reportsour current interpretation of the infrared spectra of oxoosmium(V1) esters. In a typical experiment, olefin diluted in cc14 (M/R = 10/1) and Os04 diluted in Ar (M/R = 10/1) were deposited on a CsI window held at 65-75 K.4 Warming to temperatures in excess of 180 K resulted in loss of matrix material and formation of a thin film of dimeric oxoosmium(V1) ester [OsOz(OCMe2CMe20)]2 (1) on the window. The infrared spectrum of this film

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Figure 1. (a) Infrared spectrum [OS~Z(OCM~ZCMC~O)]Z formed from wanningcodcpositedCCL/TME(10/1) andAr/Os1804 (-959boxygen18; 10/1) to >180 K. (b) Same as (a) but using O S ' ~ - ~(60% * O ~oxygen18). (c) Same as (a) but using natural-abundance 0 9 0 4 . Tabk I. Infrared Absorptions (cm-l) for [OSOZ(OCM~~CM~ZO)]Z (1)' film (I6O) film (l8O) film (180) KBr lit. lit. obsd obsd calcdd pellet P O I b assgnt' ~~

1 0

588 636 663 720 754 864 949 987 1125

563 614 634 69 1 731 840 937 1125

557 603 628 682 714 819 899 935 1098c

591 634 661 718 7 50 863 948 992 1128

588

565

655

617

08202

ring def

oszoz

ring def ring dcf

860

839

os-oc

982 1122

932 1121

O s 4 str CHj def

I, Bands to the blue of 1130 cm-I not tabulated. Reference 3. This work. Based on diatomic 0s-O. Based on diatomic (2-0. 4

Table II. Infrared Absorptions (cm-I) for OsO(OCMezCMe20)2 (210

(Figure IC) is nearly identical with that of an independently prepared sampleS (KBr pellet; see Figure 2b) and compares favorably with the literature values3 (Table I) for the reported absorptions. Additional absorptions not mentioned in the literature are reported in Table I. The spectrum obtained on oxygen-18 substitution is shown in Figure la. In general, all bands higher in energy than 1000 cm-1 show negligible isotopic shifts, while those of lower energy all show significant shifts (22-50 cm-I). In particular, the strong bandat 1125cm-',previouslyassigned tov(C-0) of theglycolate, is clearly a strictly hydrocarbon vibration. The strong band at 987 cm-1 shifts 50 cm-l, in good agreement with an absorption involving only osmium and oxygen. The doublet pattern at 987 t The Scripps Research Institute.

t University of Virginia.

(1) Schraer, M. Chem. Rev. 1980, 80, 187-213.

(2) McGrath, D. V.; Brabson, G. D.; Andrews, L.;Sharpless, K. B.

Manuscript in preparation.

(3) Collin, R. J.; Jones, J.; Griffith, W. P. J. Chem. SOC.,Dalton Trans. 1974, 1094-1097. (4) Typical ratios of OsO,/TME/CCL were approximately 1/1.5/20. ( 5 ) Criegec, R. Justus Liebigs Ann. Chem. 1936,522,75-96. Criegee, R. Ibid. 1942. 550, 99-133.

0020- 166919311332-4164S04.oOlO

KBr pcllet

assgnt

KBr pellet

632 7 10 72 1 736 824

ring def ring def ring def ring def

86 1 948 979 1123

a

assgnt 0s-O-c

0 8 4 str CH3 def

Bands to the blue of 1 130 cm-I not tabulated.

and 935 cm-I in the mixed-isotope spectrum (Figure 1b) confirms the presence of only one oxygen in the transition, consistent with a terminal O s 4 stretch. The remaining strong band at 864 cm-' has been previously assigned to a v(C-C) of the ligand. The isotopic shift of 24 cm-1 for this band, however, while not sufficient magnitudefor a strictly O s 4 or C-O vibration, indicates strong oxygen character in this transition. In the mixed-isotopic spectrum (Figure 1b) this band appears as a triplet, attesting to the involvement of two equivalent oxygen atomsin this vibration. We thereforeassign this transition to a stretching frequency in the glycolate ring. Of the remaining peaks in the 800-500-~m-~region, the 754-, 720-, and 636-cm-1 bands are previously unassigned. All three of these bands exhibit 0 1993 American Chemical Societv

Inorganic Chemistry, Vol. 32, No. 19, 1993 4165

Notes

ring. Those at lower energy more likely arise from bending motions within the ring rather than stretching motions, as supported by calculations on the monomeric monoglycolate of ethylene.6

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The original tentative assignment3of the band at ca. 660 cm-l to the central Os202 bridge was based on its necessary absence in the spectrum of the monomeric diester (2) (Figure 2a, Table 11) as well as its large shift (655 to 617 cm-l) on l*Osubstitution. This large isotopic shift is based on an incorrect assignment of peaks. We believe the correct correlation to be as shown in Table I (663 to 634 cm-l and 636 to 614 cm-l). The alternative assignment would require an isotopic shift of 49 cm-', on the basis of our data, for the 663-cm-l band, while the maximum expected shift for an Os-0 stretching band at 660 cm-l is 35 cm-l. The observed shift of 29 cm-l is in reasonably close agreement with the expected value. The weak band at 588 cm-l is also tentatively assigned to a v(Os-0) stretch3 This band exhibits a rather large l*O isotopic shift of 25 cm-l (calculated 31 cm-l) and is reassigned to the Os202 ring. Our current reassignment of the infrared data for [OsOz(OCMe2CMe20)]2 should be general for the similar absorptions of other dimeric oxoosmium(V1) ester^.^ We have used it as a basis for the identification of intermediates in the osmylation reaction which we have observed by infrared spectroscopy in lowtemperature matrices2

b

1400

1200

1000

800

600

em-'

Figure 2. Infrared spectra (KBr pellet) of (a) [OeO(OCMe2CMe20)2] and (b) [Os02(OCMezCMe20)]2prepared as in ref 5.

isotopicshifts and mixed-isotopic patterns similar to the 864-cm-l band, and hence can be assigned to vibrations in the glycolate

Ackoowledgment. The authors wish to thank Prof. M. G. Finn for helpful discussions and Ms. Wendy Saffell for technical assistance. This work was supported by grants from the National Institutes of Health (GM-28384) and the National Science Foundation (CHE-89:03218 and CHE-9 1:22556). ( 6 ) Norrby, P.0.;Kolb, H. C.; Sharpless, K. B. Unpublished rcsults.

(7) Griffith, W. P.;Raub, C. J. In Gmelin Handbuch der Anorganischen Chemie; Swars, K., Ed.;Springer-Verlag: New York, 1980; Osmium Suppl. Vol. 1, pp 186208.